Separation and determination of amygdalin and unnatural neoamygdalin in natural food supplements by HPLC-DAD

ABSTRACT

This work is focused on separation and determination of amygdalin and its unnatural form neoamygdalin in natural food supplements. Reversed-phase high-performance liquid chromatography with a high-stability silica-based column with C₁₈ functional group has been used for solving this problem. The effect of the mobile phase composition as well as the column temperature on the separation of the amygdalin epimers has been investigated. Isocratic elution using a mobile phase composed of 0.05% aqueous formic acid and acetonitrile achieved the required separation within 17 min. Under optimum chromatographic conditions, the developed method was validated and was applied for the determination of amygdalin epimers in natural food supplements containing apricot or peach kernels. A simple extraction method using methanol as an extractant supported by an ultrasonic bath was used with recovery in the range of 94.8% to 104.3%. The limit of detection and limit of quantification values for R-amygdalin were 0.13 mg/L and 0.40 mg/L, respectively. The developed method proved to be precise with the intra-day and inter-day relative standard deviation values less than 2.23%.

KEYWORDS:

• Amygdalin
• neoamygdalin
• cyanogenic glycosides
• food supplements
• high performance liquid chromatography
• separation

Declaration of interest statement

The authors declare no conflict of interest.

Additional information

Funding

This work was generously supported by the grant of projects MŠ SR VEGA [1/0678/19] and APVV-[17-0318].